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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257792Generated: November 2, 2026

Hydrochloric Acid → (6-Methylpyridin-3-yl)methanol

https://huagongshe.com/reaction/257792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantMethyl 6-methylnicotinateHCID 231548—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventTolueneHCID 1140—
Product(6-Methylpyridin-3-yl)methanolHCID 1122878822.1%

Reaction Conditions

Temperature-78 °C

Reaction Steps

5-Methoxycarbonyl-2-methyl-pyridine (3.0 g, 19.8 mmole) was dissolved in toluene (60 ml) and cooled to -78° C. To this solution, a 39.7 ml of a solution of 1M diisobutylaluminum hydride in toluene was added dropwise. The reaction mixture was stirred for 1 hour at -78° C., allowed to warm to room temperature and stirred for an additional 18 hours. Methanol (8 ml) was then added dropwise at room temperature to the reaction mixture. The mixture was stirred until a thick gel was formed. 1N HCl (10 ml) was added to dissolve the gel. The resulting phases were separated, the organic phase was extracted in ethyl acetate and dried over MgSO4. The solvents were removed yielding crude 5-hydroxymethyl-2-methylpyridine (540 mg) as an oil, which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05264437
Source datasetuspto-grants-1993_11
ORD IDord-ef3f500433cb4cc3a0d9c6758f3fbccc
Source noteuspto-grants-1993_11